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Molecular detection of Angiostrongylus vasorum in gastropods in Surrey, UK

  • L. Hicklenton
  • M. BetsonEmail author
Open Access
Helminthology - Short Communication

Abstract

Surrey, a county in southern England, is a hot spot for angiostrongylosis in domestic dogs but there have been no investigations into the intermediate hosts of Angiostrongylus vasorum in this area. This study aimed to determine the prevalence of A. vasorum in gastropods in Guildford, the most populous town in Surrey, and to ascertain which gastropod species can act as intermediate hosts for A. vasorum. Gastropods (n = 97) were sampled in six locations, representing urban, suburban and rural environments, and identified to species based on morphological features. A PCR assay was used to detect A. vasorum DNA in gastropod tissue and the species of infected specimens was confirmed by sequencing of mitochondrial genes. 4.1% (4/97) of sampled gastropods and 9.1% (4/44) of sampled slugs were A. vasorum positive. Infected gastropod species were Arion rufus (n = 3) and Deroceras invadens (n = 1), the first description of the latter species as a potential intermediate host for A. vasorum. Two infected slugs were sampled in urban environments and two in suburban environments. The results demonstrate that there is a risk of transmission of A. vasorum to domestic dogs from the gastropod population in urban and suburban areas of Guildford.

Keywords

Angiostrongylus vasorum Gastropod Deroceras invadens Arion rufus 

Introduction

The lungworm Angiostrongylus vasorum causes the serious and potentially fatal disease angiostrongylosis in domestic dogs (Elsheikha et al. 2014). It can also infect wild carnivores, such as red foxes, which are important reservoir hosts. In the UK, there are established hyperendemic foci of the parasite in Wales and southeast England and newer endemic foci in the north of England and Scotland (Helm et al. 2009; Kirk et al. 2014). Angiostrongylus vasorum has an indirect lifecycle with larval development taking place within a gastropod intermediate host. Dogs are infected through ingestion of gastropods carrying infective L3 larvae. A number of gastropod species have been implicated as intermediate hosts for A. vasorum in the UK (Aziz et al. 2016; Helm et al. 2015; Jefferies et al. 2009; Patel et al. 2014). Surrey, a county in southern England (population 1.1 million), is a hot spot for angiostrongylosis in domestic dogs (Chapman et al. 2004; Kirk et al. 2014). To date, there have been no investigations into the intermediate hosts of A. vasorum in this area. This study aimed to determine the prevalence of A. vasorum in gastropods in the area of Guildford, the most populous town in Surrey, and to ascertain which gastropod species can act as intermediate hosts for A. vasorum.

Materials and methods

A total of 97 gastropods were collected from six sites around Guildford in Autumn 2016. Collection sites were chosen based on accessibility and to represent urban, sub-urban and rural environments. Urban sites were in built up areas such as housing estates along the sides of paths and roads. Suburban sites were in open areas such as parks surrounded by built up areas. Rural sites were away from built up areas and included woodland. Gastropods were collected using forceps (and a torch if needed) between the hours of 17:00 and 11:30 and were found by looking on the ground, in hedgerows and in the undergrowth. Gastropods were identified to species using morphological keys (Kerney and Cameron 1994; Rowson et al. 2014a) and then frozen at − 20 °C.

DNA was extracted from 10 to 20 mg of gastropod foot tissue using the DNeasy Blood and Tissue kit (Qiagen). Angiostrongylus vasorum DNA was detected by PCR using the AvasF and AvasR primers (Helm et al. 2009). For molecular identification of A. vasorum-positive gastropods, cytochrome c oxidase subunit I (COI) and 16S rDNA genes were amplified using LCO1490 and HCO2198 (Folmer et al. 1994) and 16S-1 and 16S-2 (Barr et al. 2009) primers, respectively. Each 25 μl PCR reaction contained 12.5 μl MyTaq HS Red mix (Bioline, London, UK), 0.4 pmole of the forward and reverse primers and 2 μl of eluted DNA. Cycling conditions were as follows: 95 °C for 1 min, then 30 cycles of 95 °C for 15 s, 55 °C (Avas)/42 °C (CO1)/50 °C (16S) for 15 s and 72 °C for 15 s. PCR products were submitted for Sanger sequencing. BLAST searches of GenBank indicated that A. vasorum positive gastropods belonged to the larger Arionidae (n = 3) and Agriolimacidae (n = 1) families. 16S sequences representing all clades of the larger Arionidae were aligned with 16S sequences of the Arionidae specimens using CLUSTALW in MEGA v6 (Tamura et al. 2007). The alignment was used to construct a neighbour joining tree based on Kimura 2-parameter distance (Rowson et al. 2014a). Bootstrapping (1000 replicates) was carried out to test branch reliability. Similar analysis was carried out for the Agriolimacidae specimen using COI sequences.

Results and discussion

The 97 gastropods collected were classified into nine families, 15 genera and 21 species (see Supplementary Table). Differentiation between certain species (e.g., Cepaea hortensis and C. nemoralis) was not always possible based on morphology. There was a significant association between gastropod family and location type (Fisher’s exact test p < 0.0001), likely due to local ecological factors such as vegetation which favour particular families. Similar slug species were sampled in Swansea and Bristol (Aziz et al. 2016), although the relative proportions of species vary in the different locations. Interestingly, some A. vasorum-negative gastropod species sampled in Guildford have been implicated as intermediate hosts for A. vasorum, suggesting that they could also play a role in local transmission (Ferdushy and Hasan 2010; Helm et al. 2015).

Four (4.1%) of the 97 gastropods examined were positive for A. vasorum infection by PCR. All were slugs, meaning that 9.1% (4/44) of slugs were A. vasorum positive. The A. vasorum prevalence in gastropods is comparable to that recorded in Glasgow (Helm et al. 2015). The prevalence in slugs is higher than in London (Patel et al. 2014) and in Bristol, and lower than in Swansea (Aziz et al. 2016). Explanations for geographical differences could include variations in gastropod density and species composition, effects of local environment on parasite transmission and methods used for A. vasorum detection.

Sequencing of mitochondrial gene regions of A. vasorum-positive gastropods revealed that three belonged to the larger Arionidae family and the one to the Agriolimacidae family. Phylogenetic analysis of 16S sequences revealed that the three Arionidae gastropods belonged to the European Arion rufus clade (Supplementary Fig. 1), whereas similar analysis of COI sequences demonstrated that the A. vasorum-positive Agriolimacidae specimen belonged to the Dercoceras invadens clade (Fig. 1) (Rowson 2016). Two positive Ar. rufus specimens were found in urban environments. The two other positive specimens were found in suburban environments. Infected Ar. rufus slugs have been reported in the UK and Europe (Aziz et al. 2016; Eckert and Lammler 1972; Ferdushy et al. 2009; Guilhon and Cens 1973; Helm et al. 2015; Patel et al. 2014). Arion rufus is a large slug species and may be more likely to be ingested by dogs than smaller species. This study represents the first report of D. invadens as a potential intermediate host for A. vasorum, although natural infections of other Deroceras species have been described (Ferdushy and Hasan 2010; Jefferies et al. 2009; Lange et al. 2018). Deroceras invadens is widely distributed throughout the UK and Europe, typically occurring in disturbed, urban and roadside sites (Rowson et al. 2014b), suggesting ample opportunities for dogs to encounter this species.
Fig. 1

Neighbour joining tree based on cytochrome oxidase I (COI) sequences representing all clades of the Agriolimacidae family. Values next to branches indicate percentage bootstrap support. The asterisk (*) indicates the Agriolimacidae specimen collected in this study

In conclusion, there is a risk of transmission of A. vasorum to domestic dogs from the gastropod population in urban and suburban areas of Guildford. In addition, a new potential intermediate host for A. vasorum has been identified. Further work is needed to confirm whether there are differences in prevalence between urban, suburban and rural areas and investigate seasonal variations in transmission risk.

Notes

Acknowledgments

We are extremely grateful to Prof Mark Fox and Dr. Jocelyn Riggins at the Royal Veterinary College for providing Angiostrongylus vasorum positive control DNA for PCR reactions.

Funding

This work was supported by the European Scientific Counsel Companion Animal Parasites (ESCCAP) and the University of Surrey.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

A University of Surrey NASPA ethical review assessment indicated that ethical review was not required. No protected gastropod species were sampled.

Supplementary material

436_2018_6191_MOESM1_ESM.pdf (19 kb)
Supplementary Fig. 1 Neighbour joining tree based on 16S sequences representing all clades of the larger Arionidae. Values next to branches indicate percentage bootstrap support. Specimens collected in this study are labelled “Guildford sample”. (PDF 19 kb)
436_2018_6191_MOESM2_ESM.pdf (279 kb)
Supplementary Table 1 (PDF 279 kb)

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Copyright information

© The Author(s) 2019

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  1. 1.School of Veterinary MedicineUniversity of SurreyGuildfordUK

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